Основные факторы воздействия ферросплавного производства на атмосферу

На основных этапах технологического процесса получения ферросилиция образуются вредные выбросы, которыми являются колошниковые газы, шлаки и пыль. В открытых электропечах образуются газы, в которых содержится большое количество пыли и оксида углерода (до 80 % по объему). При этом оксид углерода смешивается с кислородом воздуха и сгорает с образованием диоксида углерода. В данной работе представлен количественный анализ пыле-газовых выбросов из открытой печи при получении ферросилиция и их содержание в атмосферном воздухе санитарно-защитной зоны предприятия «Юргинские ферросплавы».At the main stages of the technological process of obtaining ferrosilicon, harmful emissions are generated, which are blast-furnace gases, slags and dust. In open electric furnaces gases are formed, which contain a large amount of dust and carbon monoxide (up to 80% by volume). At the same time, carbon monoxide mixes with air oxygen and burns to form carbon dioxide. In this paper, a quantitative analysis of dust-gas emissions from an open furnace during the production of ferrosilicon and their content in the atmospheric air of the sanitary protection zone of the OAO Yurginsky Ferroalloys OJSC is presented

The choice of the reliability model of technical systems in the Mathcad package based on operational data

The subject of the research includes selection procedures, which allows determining the most adequate reliability model. Various goodness-of-fit tests and information criteria are objects of the research. Work objective is to select from predefined set the reliability model which represents given failure data sample best, by application of various statistical and information criteria

Combined proton NMR wideline and NMR relaxometry to study SOM-water interactions of cation-treated soils

Focusing on the idea that multivalent cations affect SOM matrix and surface, we treated peat and soil samples by solutions of NaCl, CaCl2 or AlCl3. Water binding was characterized with low field 1H-NMR-relaxometry (20 MHz) and 1H wideline NMR spectroscopy (400 MHz) and compared to contact angles. From 1H wideline, we distinguished mobile water and water involved in water molecule bridges (WaMB). Large part of cation bridges (CaB) between SOM functional groups are associated with WaMB. Unexpectedly, 1H NMRrelaxometry relaxation rates suggest that cross-linking in the Al-containing peat is not stronger than that by Ca. The relation between percentage of mobile water and WaMB water in the context of wettability and 1H NMR relaxation times confirms that wettability controls the water film surrounding soil particles. Wettability is controlled by WaMB-CaB associations fixing hydrophilic functional groups in the SOM interior. This can lead to severe water repellency. Wettability decreases with increasing involvement of functional groups in CaB-WaMB associations. The results demonstrate the relevance of CaB and WaMB for the dynamics of biogeochemical and hydrological processes under field conditions, as only a few percent of organic matter can affect the physical, chemical, and biological functioning of the entire 3-phase ecosystem

NMR and Raman Scattering Studies of Temperature- and Pressure-Driven Phase Transitions in CH3NH2NH2PbCl3 Perovskite

Three-dimensional methylhydrazinium (CH3NH2NH2+, MHy+) lead halides, related to the famous methylammonium (CH3NH3+, MA+) and formamidinium (CH(NH2)2+, FA) perovskites, are attractive optoelectronic materials crystallizing in polar structures. In this work, temperature-dependent 1H and 207Pb magic-angle spinning (MAS) NMR, Raman as well as high-pressure Raman studies of CH3NH2NH2PbCl3 (MHyPbCl3) are reported. Raman spectroscopy reveals many similarities between phonon properties of MHy lead halides and the MA and FA analogues. In particular, these families of compounds show an increase in wavenumber of cage modes when large I- ions are replaced by smaller Br- and then Cl- ones. They also show strong sensitivity of the CH3 torsional mode on size of the cavity occupied by MHy+ cation that decreases with decreasing size of the halide anion. The cage modes of MHyPbCl3 are, however, observed at significantly lower wavenumbers than similar modes of MAPbCl3 and FAPbCl3, indicating higher softness of MHyPbCl3. Temperature-dependent Raman and NMR studies demonstrate that the MHy+ cations in MHyPbCl3 are significantly less affected by the temperature-induced phase transition than the Pb-Cl framework. This suggests a displacive type of the phase transition dominated by tilting and deformation of the PbCl6 octahedra. Analysis of the 207Pb MAS NMR spectra reveals the presence of two differently distorted PbCl6 octahedra and diminishing (increasing) distortion of the less (more) distorted octahedra in the high-temperature phase. Pressure-dependent Raman studies reveal the presence of a single first-order pressure-induced phase transition between 0.72 and 1.27 GPa. Analysis of the spectra indicates that the driving forces for the pressure-induced phase transition in MHyPbCl3 are tilting and distortion of the PbCl6 octahedra accompanied by reorientation of MHy+ cations. Raman spectra do not show evidence of any additional phase transition or amorphization up to 6.95 GPa

Synthesis, Crystal Structure, and Solid-State NMR Investigations of Heteronuclear Zn/Co Coordination Networks - A Comparative Study

Synthesis and solid-state NMR characterization of two isomorphous series of zinc and cobalt coordination networks with 1,2,4-triazolyl benzoate ligands are reported. Both series consist of 3D diamondoid networks with four-fold interpenetration. Solid-state NMR identifies the metal coordination of the ligands, and assignment of all 1H and 13C shifts was enabled by the combination of 13C editing, FSLG-HETCOR spectra, and 2D 1H–1H back-to-back (BABA) spectra with results from NMR-CASTEP calculations. The incorporation of Co2+ replacing Zn2+ ions in the MOF over the full range of concentrations has significant influences on the NMR spectra. A uniform distribution of metal ions is documented based on the analysis of 1H T1 relaxation time measurements

Effects of Cr Doping and Water Content on the Crystal Structure Transitions of Ba2In2O5

Temperature dependent crystal structure alterations in the brownmillerite type material Ba2In2O5 play a fundamental role in its applications i photocatalytic CO2 conversion; ii oxygen transport membranes; and iii proton conduction. This is connected to a reversible uptake of up an equimolar amount of water. In this study, in situ X ray and neutron diffraction were combined with Raman spectroscopy and solid state nuclear magnetic resonance experiments to unravel the effects of Cr doping and water content on the crystal structure transitions of Ba2In2O5 H2O x over a wide temperature range 10 K lt; T lt; 1573 K, x lt; 1 . A mixture of isolated and correlated protons was identified, leading to a highly dynamic situation for the protons. Hence, localisation of the protons by diffraction techniques was not possible. Cr doping led to an overall higher degree of disorder and stabilisation of the tetragonal polymorph, even at 10 K. In contrast, a further disordering at high temperatures, leading to a cubic polymorph, was found at 1123 K. Cr doping in Ba2In2O5 resulted in severe structural changes and provides a powerful way to adjust its physical properties to the respective applicatio

Режим работы электрооборудования на тепловой станции мощностью 520 МВт

В данной выпускной квалификационной работе была спроектирована электрическая часть конденсационной электрической станции. Были рассчитаны режимы ее работы и в программе "мустанг был смоделирован самозапуск двигателей собственных нужд.In this final qualification work, the electrical part of the condensation power plant was designed. Its modes of operation were calculated and the self-launching of self-propelled engines was modeled in the Mustang program

Structure and Ionic Conductivity in the Mixed-Network Former Chalcogenide Glass System [Na2S]2/3[(B2S3)x(P2S5)1–x]1/3

Glasses in the system [Na2S]2/3[(B2S3)x(P2S5)1–x]1/3 (0.0 ≤ x ≤ 1.0) were prepared by the melt quenching technique, and their properties were characterized by thermal analysis and impedance spectroscopy. Their atomic-level structures were comprehensively characterized by Raman spectroscopy and 11B, 31P, and 23Na high resolution solid state magic-angle spinning (MAS) NMR techniques. 31P MAS NMR peak assignments were made by the presence or absence of homonuclear indirect 31P–31P spin–spin interactions as detected using homonuclear J-resolved and refocused INADEQUATE techniques. The extent of B–S–P connectivity in the glassy network was quantified by 31P{11B} and 11B{31P} rotational echo double resonance spectroscopy. The results clearly illustrate that the network modifier alkali sulfide, Na2S, is not proportionally shared between the two network former components, B and P. Rather, the thiophosphate (P) component tends to attract a larger concentration of network modifier species than predicted by the bulk composition, and this results in the conversion of P2S74–, pyrothiophosphate, Na/P = 2:1, units into PS43–, orthothiophosphate, Na/P = 3:1, groups. Charge balance is maintained by increasing the net degree of polymerization of the thioborate (B) units through the formation of covalent bridging sulfur (BS) units, B–S–B. Detailed inspection of the 11B MAS NMR spectra reveals that multiple thioborate units are formed, ranging from neutral BS3/2 groups all the way to the fully depolymerized orthothioborate (BS33–) species. On the basis of these results, a comprehensive and quantitative structural model is developed for these glasses, on the basis of which the compositional trends in the glass transition temperatures (Tg) and ionic conductivities can be rationalized. Up to x = 0.4, the dominant process can be described in a simplified way by the net reaction equation P1 + B1 P0 + B4, where the superscripts denote the number of BS atoms for the respective network former species. Above x = 0.4, all of the thiophosphate units are of the P0 type and both pyro- (B1) and orthothioborate (B0) species make increasing contributions to the network structure with increasing x. In sharp contrast to the situation in sodium borophosphate glasses, four-coordinated thioborate species are generally less abundant and heteroatomic B–S–P linkages appear to not exist. On the basis of this structural information, compositional trends in the ionic conductivities are discussed in relation to the nature of the charge-compensating anionic species and the spatial distribution of the charge carriers